Canonical Allele Identifier: CA1168547981
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56385083C= , CM000663.2:g.56385083C= GRCh38
NC_000001.10:g.56850755C= , CM000663.1:g.56850755C= GRCh37
NC_000001.9:g.56623343C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641109.1:c.759+93803G= ENSP00000493138.1:n.759+93803G=
ENST00000641346.1:c.366+15011G=
ENST00000641415.1:c.192+98180G=
ENST00000641494.1:c.378+98180G=
ENST00000642129.1:c.768+98180G=